Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.1410558A= , CM000672.2:g.1410558A= | GRCh38 |
| NC_000010.10:g.1452753A= , CM000672.1:g.1452753A= | GRCh37 |
| NC_000010.9:g.1442753A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381312.6:c.101-31398T= MANE Select | ENSP00000370713.1:n.101-31398T= | |
| ENST00000381312.5:c.101-31398T= | ENSP00000370713.1:n.101-31398T= | |
| NM_018702.3:c.101-31398T= | NP_061172.1:n.101-31398T= | |
| XR_930468.1:n.449-31398T= | ||
| NM_018702.4:c.101-31398T= MANE Select | NP_061172.1:n.101-31398T= |